Clinical Research Associate Jobs in France

Clinical Research Associate at IQVIA’s France RDS team, responsible for monitoring oncology clinical trials across multiple sponsors. Day‑to‑day duties include site visits, training delivery, compliance oversight, and data query resolution to ensure protocol integrity.

Clinical Research Associate I to monitor study sites, ensure data integrity, conduct visits, manage SAE reporting, support QA, travel required, 6 months experience, English fluency, regulatory knowledge, driver license.

IQVIA Biotech partners with visionary biotech companies to accelerate clinical development from early phase to global registrational studies. The Clinical Research Associate monitors sites, drives recruitment, manages protocol training, and ensures GCP/ICH compliance while maintaining TMF and ISF records.

Fortrea seeks a Clinical Research Associate I to manage site operations, monitor trials, ensure protocol compliance, review CRFs, handle SAE reporting, and train new staff. Requires 6 months related experience, English fluency, matrix environment proficiency, and a valid driver's license.

IQVIA Biotech partners with visionary biotech companies to accelerate clinical development from early phase through global registrational studies. The Clinical Research Associate conducts site monitoring visits, manages recruitment plans, ensures regulatory compliance, and maintains trial documentation to support study execution.

Clinical Research Associate II – a role that bridges science and solutions, overseeing global clinical trials from site management to data integrity. The position requires a solid grasp of ICH‑GCP, clinical monitoring, and regulatory compliance, with a focus on detail, documentation, and effective communication.

Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.

Engage in structured training to gain knowledge and skills for independent clinical monitoring visits per protocol, SOPs, GCP, and regulatory requirements. Perform site monitoring, training, quality evaluation, data tracking, documentation, and project support under supervision.

IQVIA offers a 6‑month internship for aspiring Clinical Research Associates in Paris. Interns receive structured training in clinical monitoring, protocol compliance, and regulatory requirements, and support site visits, data management, and documentation under supervision.

Clinical Research Associate team at IQVIA France drives oncology clinical trials by conducting site monitoring visits, administering protocol training, and ensuring GCP compliance. The role manages study progress, maintains TMF/ISF, generates visit reports, and collaborates with cross-functional teams to resolve data queries.

Global Clinical Operations (GCO) at Allucent drives clinical trial execution for biopharma partners. The CRA II/Sr. CRA independently monitors investigational sites across France, ensures protocol and GCP compliance, builds strong site relationships, and mentors junior CRAs.

Clinical Operations at Worldwide Clinical Trials is building a global CRO that innovates in oncology and hematology. The Senior Clinical Research Associate drives site qualification, monitoring, and close‑out visits, mentors junior CRAs, and ensures protocol compliance and data integrity.

Inhouse Clinical Research Associate (IHCRA) at Novotech supports the clinical team in France, ensuring compliance with ICH GCP, local regulations, and company SOPs. The role coordinates Trial Master Files, manages the Clinical Trial Management System, and assists with site visits, IRB submissions, and document archiving.

IQVIA’s Clinical Research team in Illkirch‑Graffenstaden and Paris drives global drug development by ensuring sites execute trials per GCP and ICH standards. The role monitors site visits, manages recruitment plans, and maintains Trial Master Files to guarantee data integrity.

IQVIA Clinical Functional Services Partnerships (FSP) team focuses on delivering high‑quality clinical research for a single sponsor, acting as the sponsor’s dedicated partner. The Experienced Clinical Research Associate manages site monitoring across France, drives recruitment plans, trains sites, and mentors junior staff while maintaining risk‑based monitoring practices.

Stryker Clinical Research team drives global clinical studies, ensuring quality and compliance across diverse therapeutic areas. As Lead CRA, you pilot site monitoring, mentor junior CRAs, and coordinate multi‑site operations, impacting study success worldwide.

IQVIA Clinical Research team conducts clinical monitoring visits to ensure study integrity and regulatory compliance. The Clinical Research Associate performs site monitoring, protocol training, quality oversight, progress tracking, and documentation while collaborating with study teams.

IQVIA Clinical Research team drives oncology trials across France. The associate conducts site monitoring visits, manages protocol compliance, and resolves data queries to ensure study integrity.

IQVIA’s Clinical Research team in Paris drives site monitoring and management to ensure compliance with GCP and ICH guidelines. The role conducts site visits, manages recruitment plans, and maintains Trial Master Files while coordinating with study teams.

Senior CRA responsible for data integrity, compliance with ICH GCP, and monitoring oncology trials remotely. Oversees protocol adherence, source data verification, IP management, and adverse event reporting.